{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T05:28:12Z","timestamp":1790400492960,"version":"4.1.0"},"reference-count":45,"publisher":"Oxford University Press (OUP)","funder":[{"DOI":"10.13039\/100000030","name":"Centers for Disease Control and Prevention","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000030","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Reports of ceftriaxone serious adverse events (SAEs), including deaths, from multiple jurisdictions during December 2024\u2013January 2025 prompted a nationwide investigation to evaluate product safety, characterize SAEs, and assess for changes in baseline adverse event occurrence via national databases.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>In February 2025, the Centers for Disease Control and Prevention issued a national call for cases, defined as SAEs involving death or cardiopulmonary resuscitation within 6 hours of ceftriaxone injection, not otherwise explained and occurring in non\u2013intensive care unit settings during September 2024\u2013August 2025. Epidemiologic and clinical data were collected by health departments and reported to the Centers for Disease Control and Prevention. Laboratory testing of ceftriaxone and lidocaine diluent was performed at Food and Drug Administration. Temporal trends in adverse events (2016\u20132019 vs 2020\u20132024) were assessed via Medicare claims and National Electronic Injury Surveillance System-Cooperative Adverse Drug Event Surveillance System analyses.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Among 31 cases identified from 27 healthcare facilities (65% outpatient) across 18 states during September 2024\u2013August 2025, all involving death or cardiopulmonary resuscitation, 12 (39%) persons died, 23 (74%) had anaphylaxis-type presentations (65% without skin\/mucosal involvement), 21 (68%) had previous ceftriaxone exposure, and 24 (77%) had cardiac comorbidities. Median age was 67 years (interquartile range: 60\u201381). Antihypertensive use was common (n = 19\/28, 68%). Product testing revealed no evidence of tampering, adulteration, endotoxin, or purity\/potency issues. National adverse event trends were stable across 2016\u20132019 and 2020\u20132024.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>SAEs, including deaths, can occur after ceftriaxone receipt. Product testing and trend analyses did not identify evidence of a new safety issue. This investigation highlights the need for ongoing vigilance for ceftriaxone SAEs and reporting to Food and Drug Administration MedWatch.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1093\/cid\/ciag521","type":"journal-article","created":{"date-parts":[[2026,9,3]],"date-time":"2026-09-03T01:48:55Z","timestamp":1788400135000},"source":"Crossref","is-referenced-by-count":1,"title":["A Multistate Investigation of Serious Adverse Events, Including Deaths, Following Ceftriaxone Injections, September 2024\u2013August 2025"],"prefix":"10.1093","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7390-8744","authenticated-orcid":false,"given":"Rebecca","family":"Pierce","sequence":"first","affiliation":[{"name":"Division of Healthcare Quality Promotion, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention , Atlanta, Georgia 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